Soft tissue attachment mechanism

ABSTRACT

A prosthesis humeral implant has a stem including a coupling element at a proximal end thereof and a head having a coupling element at a distal portion thereof for coupling to the stem portion coupling element. The head has a bearing surface portion for articulating on a prosthetic glenoid and a base portion. A soft tissue attachment element has an L-shape with a mounting flange portion of the L-shape extending and clamped between the bearing portion and base portion. The soft tissue attachment portion has a portion extending proximally from the mounting flange portion. The soft tissue attachment element mounting portion is captured between the head bearing portion and base portion preferably by clamping or being permanently attached to one of the base or bearing portions during manufacture.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No.12/644,297, filed on Dec. 22, 2009, which is a continuation-in-part ofU.S. application Ser. No. 12/551,692, filed on Sep. 1, 2009, thedisclosures of which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

Certain surgical procedures such as oncology surgery and major revisionsurgery require the resection of the proximal humerus where criticalsoft tissues (i.e. rotator cuff) attach to the bone. It is typical inthese surgeries to bring previously detached tendons to the implant andsuture them to the prosthesis. Soft tissue attachment is critical tomaintaining movement about the joint and preserving joint stability. Ithas been difficult to obtain secure attachment of these soft tissues toprostheses for multiple reasons.

First, in natural attachment to bone, there is a transition region ofsoft tissue to bone (i.e. muscle-tendon-bone) that changes graduallyfrom flexible to rigid. In the reattachment of soft tissue toprosthesis, this transition region is often lost and failure oftenoccurs due to the abrupt change from soft tissue to very rigid metalimplants.

Second, in certain procedures resection of surrounding soft tissuesalong with bony resections are required (i.e. resection to obtainadequate surgical margins during the removal of bone cancer such asosteosarcoma or where bone loss is significant from multiple revisionsurgeries). This soft tissue resection often leaves the remaining softtissues too short to reach their original attachment sites, even ifadequate methods of attachment directly to metal were available.

Currently, several methods are used to create a functional bridgebetween soft tissue and prostheses. These methods have exhibited limitedsuccess. Where there exists enough length for the soft tissue to reachthe prosthesis, the soft tissue is often sutured directly to theprosthesis. Advances have been made in the material and surfacetreatment of the attachment sites (i.e., the use of porous or foammetals) to improve and promote the in-growth of soft tissue aftersurgery. However, the relative stiffness of these attachment sitescompared to the soft tissue being attached continues to be a limitingfactor in the end strength of the tissue/implant interface.

In some joints, when soft tissue length is not adequate to reach thenatural attachment site on the prosthesis, graft is sometimes used tocreate a bridge. Autograft (via transplant or flap) can help to provideadditional functional length of the soft tissue, but does not addressthe stiffness issue. Also, function of the graft host site is alsoreduced. Furthermore, in the proximal humerus, there are not significantneighboring structures to create substantial tissue flaps for coverageand augmentation of tissue length. Allograft is also an option, howeveragain stiffness is not addressed and known issues of rejection and/orlack of integration with the graft tissue exist. Synthetic materialssuch as aorta-graft have been used to create a sleeve or bridge betweenthe prosthesis and bone. This can address the stiffness issue at theattachment soft tissue attachment site, however the lack of directintegration of the synthetic material with the prosthesis means thatlong term loads must be borne by sutures or other attachment mechanisms.As a result, failure of the interface may merely move from themuscle/graft interface to the graft/prosthesis interface.

Typical soft tissue attachment to a humeral prosthesis are shown in U.S.Pat. Nos. 3,803,641, 5,330,531 and 6,398,812 as well as U.S. PatentApplication Publication No. 2007/0078516.

In all of the above cases, the preparation and attachment of all ofthese grafts requires significant time and effort during the surgicalsetting, which exposes the patient to additional operating room (OR)time in what may be an already lengthy surgical procedure.

BRIEF SUMMARY OF THE INVENTION

One aspect of the humeral head to soft tissue attachment mechanism ofthe present invention creates a prosthesis that includes an attachmentsite that is less rigid than the prosthesis itself to provide a morenatural transition region for attachment. Additionally, by extendingfrom the prosthesis at or near the natural soft tissue attachment site,the mechanism provides the additional length needed in the event that aportion of the soft tissue needed to be resected as well. In thehumerus, this site is distal of the humeral head. It is envisioned thatthe prosthesis and attachment mechanism could either be monolithic or bemodular, providing surgical options if needed.

In another aspect, in a monolithic structure, the attachment materialcould be compression molded or selectively laser melted into the metalhumeral head or any suitable manufacturing means.

It is yet an additional aspect that, in a modular structure, theattachment material could be placed between a two piece humeral headwhich pieces are subsequently attached together. These could be attachedrigidly during manufacturing and sold as one piece or sold separatelyintended to be attached at the time of surgery.

Although not shown explicitly, it is intended that the attachmentmechanism could be provided to the surgeon in an intentionally longlength so that the surgeon could trim and shape the protrusion to obtainan optimized attachment site for both size and soft tissue tension.

In one aspect of the invention the attachment mechanism could either besynthetic, biologic, synthetic/biologic composite or hybrid material.The choice of material for attachment would be largely dictated by therequirements of the particular soft tissue being addressed from theperspective of in-growth potential, natural loading requirements,healing potential and other factors.

The material (whether synthetic or biologic) could benefit (depending onsite) from being biodegradable or bioresorbable such that over time, itis replaced by the natural soft tissue. In this way, the soft tissuehealing would have the opportunity to create a natural soft-to-hardtransition region with the prosthesis.

It is also considered that the material (whether synthetic or biologic)could benefit (depending on site) from being porous, especially at thesite of soft tissue attachment to promote in-growth. It is alsoenvisioned that technologies could be applied to vary the porositythroughout the attachment mechanism throughout its length (to createvarying material properties which would create a more natural transitionregion) or throughout its cross section (to limit the in-growth ofunwanted tissues).

Some examples of suitable synthetic materials are Dacron, polytetrafluorethylene (PTFE), Leeds-Keio (L-K) artificial ligament, Texturizedor Open-weave poly(ethylene terephthalate), waterswolenpoly(2-hydroxyethyl methacrylate), polydioxanone (PDO), PDO/ElastinWeave), polyurethane (PU), aromatic porous polyurethane, poly-(L-lacticacid) (PLLA), and Polyetheratherketone (PEEK). Some examples of biologicor hybrid composite materials could be allograft or xenograft tendon orligament, small-intestinal submucosa (SIS), collagen, cell seededcollagen matrices, hydrogels, Chitosan or other known cell scaffoldmaterials.

A further aspect of the invention provides a method of securing softtissue to a prosthetic bone implant. The method may comprise implantinga joint bone prosthesis adjacent to a joint at or near a natural softtissue attachment site, the prosthesis connected to a one-piece softtissue attachment component. The method may also include suturing thesoft tissue attachment component to the natural soft tissue withfilaments.

In one embodiment of the method, the step of attaching the soft tissueattachment component to natural soft tissue may include fixing thenatural soft tissue between the prongs of a forked end of the softtissue attachment component. In another embodiment, attaching the softtissue attachment component to natural soft tissue may include suturingthe natural soft tissue to the soft tissue attachment component withfilaments connected to the end of the soft tissue attachment component.Other embodiments may include attaching the soft tissue attachmentcomponent to a bony structure by implanting a plug into the bonystructure, wherein the plug is connected to the soft tissue attachmentcomponent, or attaching the soft tissue attachment component to a bonystructure by fixing a replacement or resurfacing component to the bonystructure, where the replacement or resurfacing component is connectedto the soft tissue attachment component.

A prosthetic humeral implant includes a stem having a coupling elementat a proximal end thereof. The implant has a head having a couplingelement at a distal portion thereof for coupling to the stem portioncoupling element. The head has a bearing portion and a base portion. Asoft tissue attachment element, having a mounting portion, extendsbetween the bearing portion and the base portion. The soft tissueattachment portion extends proximally from the base portion. A clamp isprovided for capturing the soft tissue attachment element mountingportion between the head bearing portion and base portion. The baseportion may have a porous surface thereon. The porous surface may extendaround a circumferential surface of the base portion. The clamp forcapturing the soft tissue mounting portion may include threaded elementsextending between the head bearing portion and base portion. The softtissue attachment element may be made of a flexible material selectedfrom the group consisting of Dacron, polytetra fluorethylene, texturizedor open-weave poly(ethylene terephthalate), waterswolenpoly(2-hydroxyethyl methacrylate), polydioxanone, PDO/Elastin weave,polyurethane, aromatic porous polyurethane, poly-(L-lactic acid),Polyetheratherketone, allograft or xenograft tendon or ligament,small-intestinal submucosa, collagen, cell seeded collagen matrices,hydrogels, and Chitosan. The soft tissue attachment element could alsobe made of metal. The humeral implant may have a tissue attachmentelement which has a planar surface forming the mounting portion. Thehumeral implant base portion may include a porous metal tissueattachment portion.

A prosthetic humeral implant includes a stem and a head coupled to thestem. The head has a base element and a bearing element slidably coupledto one another. An anti-rotation element is mounted on one of the baseelement and bearing element preventing rotation therebetween. A softtissue attachment element has a first portion captured between the baseelement and the bearing element and a second portion extending from thebase element towards the bearing element. A clamp is provided for movingthe base element towards the bearing element to capture the soft tissueattachment element therebetween. The base portion may have a poroussurface thereon wherein the porous surface extends around thecircumference of the base portion

As used herein when referring to bones or other parts of the body, theterm “proximal” means close to the heart and the term “distal” meansmore distant from the heart. The term “inferior” means toward the feetand the term “superior” means toward the head. The term “anterior” meanstoward the front part or the face and the term “posterior” means towardthe back of the body. The term “medial” means toward the midline of thebody and the term “lateral” means away from the midline of the body.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 a is an isometric view of a prosthetic tibial implant includingthe soft tissue attachment device of the present invention;

FIG. 1 b is a lateral view of the tibial implant including soft tissueattachment device of the present invention;

FIG. 1 c is an anterior view of the prosthetic tibia shown in FIGS. 1 aand 1 b;

FIG. 1 d is a top view of the prosthetic tibial components of FIGS. 1 athrough 1 c showing the superior surfaces thereof;

FIG. 2 a is a prosthetic tibia including a modular soft tissueattachment device of the present invention;

FIG. 2 b is a lateral view of the tibia of FIG. 2 a showing the softtissue attachment device spaced anteriorly of the tibia;

FIG. 3 a is an alternate prosthetic component having a receptacle forreceiving soft tissue as shown;

FIG. 3 b is an anterior view of the prosthetic component of FIG. 3 a;

FIG. 4 a is an isometric view of a prosthetic tibial implant having yetan additional alternate embodiment of the soft tissue attachment deviceof the present invention;

FIG. 4 b is an anterior view of the prosthetic tibial component of FIG.4 a;

FIG. 4 c is a lateral view of the prosthetic tibial components of FIGS.4 a and 4 b;

FIG. 4 d is a top view of the prosthetic tibial component of FIGS. 4 athrough 4 c joining the superior surface of the component;

FIG. 5 a is an isometric view of yet another alternate soft tissueattachment device of the present invention showing a tibial prosthesiswith a proximally extending soft tissue attachment component withresurfacing element;

FIG. 5 b is a posterior view of the prosthetic tibial component of FIG.5 a;

FIG. 5 c is a lateral view of the prosthetic tibial component of FIGS. 5a and 5 b;

FIG. 5 d is an anterior view of the soft tissue attachment device ofFIGS. 5 a-5 c;

FIG. 5 e is a top view of the prosthetic femoral components of FIGS. 5a-5 d;

FIG. 6 a is an isometric view of yet another embodiment of the softtissue attachment device of the present invention;

FIG. 6B is an isometric view of the embodiment of FIG. 6A with the softtissue attachment element disassembled from the prosthetic tibia;

FIG. 7 a is a front view of an additional embodiment of the presentinvention;

FIG. 7 b is an isometric view of the ultimate embodiment of FIG. 7A withthe prosthetic patellar element removed; and

FIG. 7 c is a posterior view of the embodiment of FIGS. 7 a and 7 b withthe prosthetic patella disassembled from the soft tissue attachmentdevice.

FIG. 8 is a view of the medially facing side of the humeral implant withsoft tissue attachment device of the present invention;

FIG. 9 is an anterior or posterior view of the humeral implant of FIG.8;

FIG. 10 is a view from the lateral side of the humeral implant of FIG.8;

FIG. 11 is a cross-sectional view of the implant of FIG. 10 along thelines A-A;

FIG. 12 is a cross-sectional view of the implant of FIG. 10 along linesB-B;

FIG. 13 is an exploded view of the humeral implant of FIG. 8;

FIG. 14 is a view from the lateral side of the humeral implant of FIG.13;

FIG. 15 is an enlarged view of the humeral head shown in FIG. 13;

FIG. 16 is a view of the medial side of the head portion of the humeralimplant of FIG. 8 showing the bearing surface and tissue attachmentelements;

FIG. 17 shows the humeral head of the humeral implant of FIG. 13 in anassembled position;

FIG. 18 is a lateral view of the humeral head of FIG. 17;

FIG. 19 is a view similar to FIG. 16 showing an alternate tissueattachment element;

FIG. 20 is an anterior/posterior view of the humeral head of FIG. 19;

FIG. 21 is a lateral view of the humeral head embodiment of FIG. 20;

FIG. 22 is an exploded view of an alternate embodiment of a humeral headincluding a tissue attachment element having suture attachment openings;

FIG. 23 shows a humeral head having a tissue attachment portion on alateral surface thereof; and

FIG. 24 is a lateral view of the assembled head component of FIG. 23.

DETAILED DESCRIPTION

Referring to FIGS. 1 a through 1 d there is shown a preferred embodimentof a prosthetic tibial component generally denoted as 10, which may bepart of modular oncology system such as disclosed in U.S. Pat. No.4,578,081. In such a system large portions of diseased bones are removedand replaced by prosthetic implants such as the proximal tibia. Thetibial prosthesis includes a proximal tibial portion 12 and a proximallyextending soft tissue attachment device 14. In the preferred embodiment,soft tissue attachment device 14 includes a stem portion 16, which iscoupled to the proximal end 18 of prosthetic tibia 12. The device 14 maybe one-piece with the proximal tibia such as by being integrally casttherewith or welded thereon. Other techniques such as Selector LaserMelting (SLM) or compression molding may also be used.

Soft tissue attachment device 14 includes first and second arms 20 and22, which form a generally U-shaped slot 24. Slot 24 is designed toreceive a portion of the patellar tendon. Arms 20 and 22 merge at ajunction 26 to form stem 16. In the preferred embodiment, the proximalsuperior facing surface of tibial prosthesis 12 is a planar surface 28.While a U-shaped slot is shown, other shape slots may also be used.

In the preferred embodiment, surface 28 includes four proximallyextending flange portions 30, 32, 34, and 36. Flange portions 30, 32,34, and 36 are designed to receive a prosthetic bearing surface which,in the preferred embodiment, is made of ultrahigh molecular weightpolyethylene (UHMWPE). However, the bearing component may be made ofother polymeric or metal materials suitable for prosthetic bearings.When a UHMWPE insert (not shown) is utilized, it may be snapped andlocked in recessed grooves 38, 40, 42, and 44 formed in flanges 30, 32,34, and 36, respectively.

Referring to FIGS. 2 a and 2 b, there is shown a modular connectionbetween the proximally extending tendon attachment device 14 and theproximal portion 18 of tibia prosthesis 12. The modular attachmentincludes a flange or plate element 40 having a pair of through holes 42for receiving screws (not shown), which engage with threaded bores 44and 46 in tibial prosthesis 12. Threaded bores 44 and 46 are preferablyformed in a recessed area 48 formed in the anterior facing surface ofthe proximal tibia portion 18. The recess preferably has a distalsurface 50, which receives a bottom surface 52 of flange portion 40 ofthe proximally extending stem portion 16 tendon attachment device 14.Surface 50 provides support for distal surface 52. As discussed above,stem portion 16 is fixedly attached to or integral with flange portion40. The stem portion 16 may be attached by welding so that the tendonattachment device 14 is made one piece with flange portion 40.

Referring to FIG. 2 b, flange portion 40 includes a proximally facingsurface 54, which engages a distally facing surface 56 on the recessedportion 48 of prosthetic tibial component 12. Thus flange portion 40,once assembled, is prevented from proximal-distal movement by surfaces50 and 56 of recess 48.

Referring to FIGS. 3 a and 3 b, there is shown an alternate method ofattaching a tendon 60. In this embodiment the plurality of filaments arewoven or stitched into soft tissue similar to suturing.

Referring to FIGS. 4 a through 4 d, there is shown yet an additionalembodiment of the proximally extending tendon attachment device of thepresent invention. In this embodiment, prosthetic tibia 12 remainsessentially unchanged with an alternate tendon attachment device 14 ahaving a stem 16 a attached to an anteriorly facing surface of proximalportion 18 of tibia prosthesis 12. The tendon attachment area includesfour spaced arms 70, 72, 74, and 76, which form U-shaped open areasfacing anteriorly and posteriorly as well as medially and laterally. Aproximally facing elongate pin 78 is provided. The four spaced arms 70,72, 74 and 76 are attached to the soft tissue in the same manner asdescribed with respect to FIG. 1 after the plug is implanted into thepatella for load sharing. Pin 78 can be cylindrical or can have othershapes.

Referring to FIGS. 5 a through 5 e, there is shown yet an additionaldesign for the proximally extending tendon attachment device wherein,again the tibial prosthetic portion 12 remains the same. However, inthis embodiment, a proximally extending tendon attachment device 14 bincludes a stem portion 16 b attached to the anteriorly facing surfaceof the tibial prosthesis 12. A resurfacing portion 80 is provided at theproximal end of the stem 16 b, which the resurfacing portion includesthree pointed pins 82, 84, and 86. Pins 82, 84, and 86 extend anteriorlyfrom an anterior surface 88 of resurfacing portion 80. The posteriorsurface of resurfacing element 80 includes a smooth portion 90, whichmay be part spherical in shape. Part spherical surface 90 may act as aprosthetic patellar surface once the patella is attached to pins 82, 84,and 86. In this embodiment, the stem 16 b and attachment device 14 b mayextend anteriorly and proximally to locate surface 90 of resurfacingportion 80 at the proper location for engaging a trochlear groove of aprosthetic femoral component (not shown).

Referring to FIGS. 6 a and 6 b there is shown an alternate embodiment inwhich a soft tissue attachment element such as a patellar tendonattachment element 200 is coupled to a prosthetic tibial component 212by clamping element 202. Attachment element 200 has a curved distalportion 204 which sits in a groove 206 formed in a recess 208 in theanterior portion of component 212. Portion 204 is clamped within recess206 by clamp 202. Clamp 202 includes a pair of apertures 210 forreceiving screws (not shown) which thread into threaded bores 214 formedin the anterior surface of component 212 in the area of recess 208. Softtissue attachment element 200 includes an anteriorly extending portion216 which forms a proximal part of curved distal end portion 204.Portion 216 fits within cut-out 218 of clamp 202 when the soft tissueattachment element 200 is assembled as shown in FIG. 6A.

Referring to FIGS. 7 a-7 c, a proximal tibial component 312 with anintegral soft tissue attachment element 300 integrally formed therewithsuch as by welding or casting. Soft tissue attachment element 300includes a proximal end 302 having a plurality of through holes 304 forreceiving the pegged posterior receiving peg elements 306 of aprosthetic patellar component 308. A small protrusion 310 is formed onthe anterior face of proximal end 302 of soft tissue attachment element300. Protrusion 310 extends into a recessed bore 312 formed on theposterior face of prosthetic patella 308. As in all of the otherembodiments the proximal surface 328 includes locking elements 314 forfixing a ultra high molecular weight polyethylene bearing surface to theproximal tibia. Such structures are well known in the art.

Referring to FIG. 8 there is shown a humeral implant assembly generallydesignated as 100 viewed medially from the center of the body. Theimplant 100 has a distal item 102 and a proximal end 104. Proximal end104 includes a typical bearing surface 106 which engages a glenoidcomponent (not shown) when used in a total shoulder replacement. In oneembodiment the bearing surface 106 is mounted on a modular proximal headelement 108 which is connected via a body element 110 to distal stemportion 102. Stem portion 102 has a tip 112 which is adapted to beinserted into the intramedullary canal of the proximal humerus such thatstem 102 is located within the canal. Stem 102 may be of any standarddesign. Preferably body portion 110 includes a conically tapered maletrunion for placement in a conically tapered female receptacle on head108. This coupling system can be seen, for example, in FIG. 11. Thetapered system can use a standard Morse type taper connection or anyacceptable connection mechanism. Attached to head 108 is a tissueattachment element 114 which extends medially and proximally towards theglenoid when the humeral implant 100 is implanted within the humerus.Referring to FIG. 9, there is shown humeral implant 100 when viewedeither anteriorly or posteriorly. As can be seen bearing surface 106 isoriented to engage a prosthetic glenoid (not shown) and tissueattachment element 114 is oriented to allow attachment of soft tissuesuch as ligaments and tendons of the shoulder. As discussed hereinbelow, a laterally facing surface 116 of head portion 108 includes abore 118 for receiving a clamping screw 118 best seen in FIG. 12. Asshown in FIG. 10 a similar screw 118 is located on the opposite anterioror posterior side of implant 100. While the humeral implant 100 isdescribed as a modular implant having separate head and stem portions,these portions could easily be combined into a one-piece design withoutdeparting from the spirit and scope of this invention.

Referring to FIG. 10, there is shown humeral implant 100 when viewedfrom laterally of the body. As such surface 116 can be viewed along withthe two screw containing bores 118. It can be seen that tissueattachment element 114 extends circumferentially around head portion 108with the exception of the distal-most portion 119 of the head 108.Distal gap 119 of tissue attachment element 114 prevents its contactwith bony anatomic structures.

Referring to FIG. 11, there is a cross-sectional view of the implant ofFIG. 10 along lines A-A. As can be seen, the proximal end of bodyportion 110 includes a conically tapered trunion 120 which is receivedwithin a conically tapered receptacle 122 in the head portion 108. Headportion 108 is preferably made in two parts. First part 124 includesbearing surface 106 and a second part 126 includes trunion receivingbore 122. A clamping interface 128 extends circumferentially around ajunction between first part 124 and second part 126. Parts 124 and 126have matching planar circumferential surfaces which may clamp together.Of course any clamping system may be utilized. Interface 128 receives amounting portion or flange 130 of soft tissue attachment element 114 asbest seen in FIG. 12. Portion 130 is connected to a flange portion 131of tissue attachment element 114.

Referring to FIG. 12 there is shown a cross-section of the prostheticimplant of FIG. 10 along the lines B-B showing bore 118 housing a screw132. As can be seen in FIG. 10, there are two screws 132 located on theanterior and posterior sides of the implant. The tightening of screw 132into threaded bore 134 of part 124 clamps portion 130 of tissueattachment element 114 in position. While threaded screws are shown, anyother method of attaching element 114 to head 108 may be utilized. Forexample, other clamping, pin, tabs, welding, press-fit, quick-connect ortaper lock.

Regarding soft tissue attachment element 114, this element may be madeof a material such as Dacron, polytetra fluorethylene, texturized oropen-weave poly(ethylene terephthalate), waterswollenpoly(2-hydroxyethyl methacrylate), polydioxanone, PDO/Elastin weave),polyurethane, aromatic porous polyurethane, poly-(L-lactic acid),Polyetheratherketone, allograft or xenograft tendon or ligament, smallintestinal submucosa, collagen, cell seeded collagen matrices, hydrogelsand Chitosan.

Referring to FIG. 13, there is shown the prosthetic humeral implant ofFIGS. 8-12 with all the parts disassembled. Stem 102 and body 110including trunion 120 are, in the preferred embodiment, monolithic,although these parts can be modularized in a well known fashion withadditional male and female tapered interconnections similar to the morsetype taper of trunion 120. Head portion 108 is shown disassembled intofirst element 124 which includes articular surface 106 and secondsection 126 which includes screw 132 extending into bore 118. Portion131 of tissue attachment element 114 is shown extending partiallycircumferentially around the interface 128 between sections 124 and 126.In the embodiment shown in FIGS. 13-15, a porous tissue attachmentsurface 136 is shown formed on an outer circumference of second section126 of head 108. Porous tissue attachment portion 136 may be a poroustitanium metal, foam metal, porous surface produced by selective lasermelting or may be a roughened surface. Any structure that provides aconductive structure to allow the natural tissue of the patient toadhere or to ingrow over time following implantation can be used. Thesesurfaces may be coated with a biological treatment such as a bonemorphogenic protein solution or be coated with hydroxapatite to enhanceor promote biologic attachment or incorporation of the shoulder jointtissue onto the implant. A bone morphogenic protein that may be utilizedis OP-1 sold by Stryker Corporation.

Referring to FIG. 15 there is an alternate embodiment of head 108 whichis the same in all respects except that first section 124 a includes aporous tissue ingrowth surface 138, which, upon assembly, is locatedadjacent porous surface 136. Porous surfaces 136 and 138 may beidentical structures as discussed above with respect to surface 136.

As can be seen in FIGS. 13 and 15 second section 126 of head 108preferably has a smooth part spherical laterally facing surface and apart rectangular medially facing protruding portion 140. The laterallyfacing surface of first portions 124 and 124 a include a rectangularrecess for receiving protruding portion 140 which recesses include apair of threaded bores 134 extending therefrom into portions 124, 124 a.The rectangular mating structure is a matter of design choice and anymating structure which prevents rotation of first portion 124, 124 awith respect to second portion 126, 126 a could be utilized. Referringto FIGS. 16-18, head 108, including second section 126 a, with tissueingrowth portion 136, is shown in an assembled condition. FIG. 16 showsa view from the medial part of the body including medially andproximally extending flange portion 131 of tissue attachment element 114which extends approximately 290° circumferentially making the angle θapproximately 70°. In a typical embodiment, the diameter d of the tissueattachment element is approximately two inches with the head 104 havinga proximal distal dimension of about 1.5 inches and a medial-lateralwidth of approximately 1.6 inches. These dimensions of course may changedepending on the implant size. In addition, the length of a tissueattachment flange portion 131 of tissue attachment element 114 may bebetween approximately 0.35 and 0.8 inches. This distance can be madelonger if the surgeon prefers.

Referring to FIGS. 19-21 there is shown an alternate embodiment of thehead 108 shown in FIGS. 16-18. In the alternate embodiment of FIGS.19-21, the tissue attachment element 114 is interrupted and, in theembodiment shown, includes four segments 150, 152, 154 and 156. Thesegments 150, 152, 154 and 156 form three interruptions 158, 160 and162. These interruptions may be located at any angle and at any desiredlength. For that matter only a single interruption in addition to gap119 can be used. The purpose of the interruptions are to have theability to attach muscles/tendons in specific locations.

Referring to FIG. 22, there is shown an alternate embodiment in whichflange 131 of soft tissue attachment element 114 includes a plurality ofsuture through holes 164. The through holes 164 may be spaced evenlyaround the circumference of tissue attachment element 114 and areadapted to allow sutures extending through soft tissue to be attached toflange portion 131 of element 114.

Referring to FIGS. 23 and 24, there is shown an alternate embodiment ofhumeral head 108 in which the elements are manufactured in one piece. Inthis embodiment, the soft tissue attachment element 114 has beencaptured within head 108 by a manufacturing process such as injection orcompression molding. In this method the soft tissue attachment elementis positioned in the mold and the implant material is compressed onto itto capture it in the head. As described previously, this embodiment mayalso have porous metal region 136.

Although the invention herein has been described with reference toparticular embodiments, it is to be understood that these embodimentsare merely illustrative of the principles and applications of thepresent invention. It is therefore to be understood that numerousmodifications may be made to the illustrative embodiments and that otherarrangements may be devised without departing from the spirit and scopeof the present invention as defined by the appended claims.

The invention claimed is:
 1. A prosthetic bone implant, the bone implantforming one side of a joint, comprising: a prosthesis; a soft tissueattachment component connected to the bone implant and extendingoutwardly therefrom and towards a joint line and extends beyond thejoint line; wherein the soft tissue attachment component is moveablewith respect to the prosthesis while connected thereto; and wherein thesoft tissue attachment component has a first end and a second end, thefirst end configured to connect to the prosthesis and the second endincluding a forked tip configured to engage a soft tissue, theconnection between the first end of the tissue attachment component andthe prosthesis allowing the connection to occur after implantation ofthe prosthetic bone implant.
 2. The prosthetic bone implant of claim 1,wherein the soft tissue attachment component has a first end and asecond end, the first end configured to attach to the prosthesis and thesecond end including a plug configured for attachment to bone.
 3. Theprosthetic bone implant of claim 1, wherein the soft tissue attachmentcomponent has a first end and a second end, the first end configured toattach to the prosthesis and the second end attached to a replacement orresurfacing element for a bony structure.
 4. The prosthetic bone implantas set forth in claim 1 wherein the first end includes a stem portionwhich is coupled to the prosthesis.
 5. The prosthetic bone implant asset forth in claim 4 wherein the stem portion is fixedly held on theprosthesis by screws.
 6. The prosthetic bone implant as set forth inclaim 4 wherein the stem portion includes a flange and the prosthesisincludes a recess for receiving the flange.
 7. The prosthetic boneimplant as set forth in claim 6 wherein the flange has a surface facingthe soft tissue attachment component second end engaging a stop surfacein the recess.
 8. The prosthetic bone implant of claim 1, wherein thesoft tissue attachment component is at least partially porous.
 9. Theprosthetic bone implant of claim 1, wherein the soft tissue attachmentcomponent has a variable porosity throughout its length or throughoutits cross section, or throughout both its length and its cross section.10. A prosthetic bone implant, the bone implant forming one side of ajoint, comprising: a prosthesis for replacing one side of a joint, theprosthesis having a bearing surface located on one side of a joint line;and a soft tissue attachment component having a flange portion fixedlyconnected to the prosthesis adjacent at a first end and extendingoutwardly therefrom beyond the joint line at a second end, the softtissue attachment component further comprises a stem portion formed as aone-piece construct with the flange portion, the stem portion having afree end with first and second arms forming a U-shaped slot, theU-shaped slot being open proximally at a free end thereof and having twomedial and lateral side openings extending from the open free end of theslot distally towards the stem portion the flange portion has aplurality of holes therethrough and the prosthesis has a recessed areawith threaded bores aligned with the holes in the flange and the flangeis held on the prosthesis with screws; wherein the soft tissueattachment component is moveable with respect to the prosthesis whileconnected thereto.
 11. The prosthetic bone implant of claim 10, whereinthe soft tissue attachment component is at least partially porous. 12.The prosthetic bone implant of claim 10, wherein the soft tissueattachment component has a variable porosity throughout its length orthroughout its cross section, or throughout both its length and itscross section.
 13. The prosthetic bone implant of claim 12 wherein thesoft tissue attachment component is formed integrally with thereplacement or resurfacing element.
 14. The prosthetic bone implant ofclaim 10 wherein the prosthesis and the soft tissue attachment mechanismare configured to be connected at the time of surgery.
 15. Theprosthetic bone implant of claim 10, wherein the soft tissue attachmentcomponent is configured to be modified by a surgeon according to thesize and tension needs of a particular procedure.
 16. The prostheticbone implant of claim 10, wherein the soft tissue attachment componentis composed at least in part of a material that is either synthetic orbiologic, or a composite of synthetic and biologic materials.
 17. Aprosthetic bone implant, the bone implant forming one side of a joint,comprising: a prosthesis; a soft tissue attachment component connectedto the bone implant and extending outwardly therefrom and towards ajoint line and extends beyond the joint line; wherein the soft tissueattachment component is moveable with respect to the prosthesis whileconnected thereto; wherein the soft tissue attachment component has afirst end and a second end, the first end configured to attach to theprosthesis and the second end including a forked tip configured toengage a soft tissue wherein the first end includes a stem portion whichis coupled to the prosthesis; and wherein the stem portion includes aflange and the prosthesis includes a recess for receiving the flange.18. The prosthetic bone implant as set forth in claim 17 wherein theflange has a surface facing the soft tissue attachment component secondend engaging a stop surface in the recess.
 19. The prosthetic boneimplant as set forth in claim 17 wherein the stem portion is fixedlyheld on the prosthesis by screws.